Catalyst system for producing polyethylene copolymers in a high temperature solution polymerization process

ABSTRACT

Catalyst system for producing ethylene copolymers in a high temperature solution process, the catalyst system comprising (i) a metallocene complex of formula (I), M is Hf or a mixture with Zr, provided that more than 50% by moles of the complex of Formula I has M=Hf, X is a sigma ligand, R are the same or different from each other and can be saturated linear or branched C 1 -C 10  alkyl, C 5 -C 10  aryl, C 6 -C 20  alkylaryl or C 6 -C 20  arylalkyl groups, which can optionally contain up to 2 heteroatoms or silicon atoms, R 1  is a C 6 -C 20 -aryl, which can be unsubstituted or substituted by one or up to 5 linear or branched C 1 -C 10  alkyl group(s), R 2  is a saturated linear or cyclic C 3 -C 20  alkyl group or a branched CR 3 R 4 R 5  group, wherein R 3  is hydrogen or an C 1 -C 20  alkyl group and R 4  and R 5  are the same or are different and can be an C 1 -C 20  alkyl group and (ii) a boron containing cocatalyst.

The present invention is related to a new catalysts system, which is able to produce polyethylene copolymers in a high temperature solution polymerization process. The new catalyst system comprises a specifically substituted, bridged hafnocene catalyst complex, comprising a cyclopentadienyl (Cp) ligand, a fluorenyl (Flu) ligand and a covalent bridge connecting the two ligands, along with a boron based cocatalyst. This combination remarkably gives rise to catalyst systems with an improved balance of solubility, productivity, comonomer incorporation ability and molecular weight capability.

Metallocene catalysts have been used to manufacture polyolefins for many years. Countless academic and patent publications describe the use of these catalysts in olefin polymerization. Metallocenes are now used industrially and polypropylenes as well as polyethylenes are often produced using cyclopentadienyl based catalyst systems with different substitution patterns.

Several of these metallocene catalysts have been described for the use in solution polymerization for producing polyethylene homo- or copolymers.

For example WO 2000024792 describes a catalyst system comprising hafnocene catalyst complex derived from A) a biscyclopentadienyl hafnium organometallic compound having i) at least one unsubstituted cyclopentadienyl ligand or aromatic fused-ring substituted cyclopentadienyl ligand not having additional substituents on said ligand, ii) one substituted or unsubstituted, aromatic fused-ring substituted cyclopentadienyl ligand, and iii) a covalent bridge connecting the two cyclopentadienyl ligands.

This bridge can be a single carbon substituted with two aryl groups, each of these aryl groups being substituted with a C₁-C₂₀ hydrocarbyl or hydrocarbylsilyl group, whereby at least one of these substituents is a linear C₃ or greater substituent.

In addition the catalyst system comprises an activating cocatalyst, which is preferably a precursor ionic compound comprising a halogenated tetraaryl-substituted Group 13 anion.

Also EP 2511305 is related to bridged Cp-Flu metallocene complexes. The C-based bridges shown in the Examples are substituted methylene bridges, whereby the substituents are the same (e.g. dimethyl, diphenyl, dibenzyl, dicyclohexyl etc) or are linked together to form a ring (e.g. cyclohexylidene).

Yano and co-workers (literatures 1 to 4) studied the effect of ligand structure on high temperature ethylene homo-polymerization and copolymerization with various Cp-Flu metallocenes.

-   1. A. Yano, M. Sone, S. Hasegawa, M. Sato, A. Akimoto, Macromol.     Chem. Phys. 1999, 200, 933. -   2. A. Yano, S. Hasegawa, T. Kaneko, M. Sone, M. Sato, A. Akimoto,     Macromol. Chem. Phys. 1999, 200, 1542. -   3. A. Yano, M. Sone, S. Yamada, S. Hasegawa, M. Sato, A. Akimoto,     Journal of Molecular Catalysis A: Chemical 2000, 156, 133. -   4. S. Hasegawa, M. Sone, M. Tanabiki, M. Sato, A. Yano, Journal of     Polymer Science: Part A: Polymer Chemistry 2000, 38, 4641.

The main teachings from this work are:

-   i) With Zr as the metal, in C2 homopolymerization and C2/C6     copolymerization, a Ph₂C bridge provides higher activity and higher     Mw compared to a Me₂C bridge -   ii) Addition of substituents on the Cp ligand does not significantly     change catalyst performance -   iii) With Zr as the metal, in C2/C6 copolymerization, addition of     methyl or tert-butyl substituents in the 2,7 positions of the Flu     ligand increases molecular weight of the copolymer but does not     affect comonomer reactivity nor catalyst productivity -   iv) With Hf as the metal, in C2/C6 copolymerization, addition of     tert-butyl substituents in the 2,7 positions of the Flu ligand     slightly increases catalyst productivity but molecular weight of the     copolymer and comonomer reactivity are hardly affected -   v) Zr complexes are more active than Hf complexes. For both the Zr     and analogue Hf complexes, a Ph₂C bridge provides higher activity     and higher Mw compared to a MePhC or Me₂C bridge -   vi) The Ph₂C(Cp)(Flu)ZrCl₂ complex give lower copolymer Mw compared     to its Hf analogue

In none of the above cited literatures and patents the simultaneous increase of solubility, productivity, molecular weight capability and comonomer incorporation ability of the catalyst system is mentioned.

Furthermore the above cited literatures and patents do not address the effect of the steric encumbrance of a bridge being composed of a C-atom substituted by an aryl group whereas the second substituent being a non-aryl substituent at higher polymerization temperature on the catalyst performance of a Hafnium complex.

However, for a process for producing ethylene copolymers to be efficient, it is important that the catalyst system used has to fulfil a set of very strict requirements. Comonomer incorporation ability for higher comonomers (comonomer reactivity), catalyst molecular weight capability (lowest achievable melt index for a given polymer density, monomer concentration and polymerization temperature) and catalyst thermal stability must ensure the production of copolymers with density down to ˜0.850 g/cm³ and a melt index MI₂ (190° C., 2.16 kg) down to ˜0.3 g/10 min with high productivity (in order to get a maximum of polyethylene produced with as low amount of catalyst as possible). Solubility of the transition metal complex in aliphatic hydrocarbons is also important to ensure optimal use of the complex in a solution process.

Although a lot of work has been done in the field of metallocene catalysts, there still remains a need to find new catalyst systems for ethylene copolymerization, which are able to produce polymers with desired properties and which have improved balance of solubility, productivity, comonomer incorporation ability and molecular weight capability.

As a consequence, the inventors set out to develop a new catalyst system having superior polymerization behaviour than the above mentioned polymerization catalyst systems regarding to solubility, productivity, comonomer incorporation ability and molecular weight capability.

The present inventors have now found a new class of olefin polymerization catalyst systems, which are able to solve the problems disclosed above. In particular, the invention combines the use of special metallocene complexes with a boron cocatalyst.

SUMMARY OF INVENTION

Thus, viewed from one aspect the invention relates to a catalyst system for producing ethylene copolymers in a high temperature solution process, the catalyst system comprising

-   -   (i) a metallocene complex of formula (I)

-   -   wherein     -   M is Hf or a mixture with Zr, provided that more than 50% by         moles of the complex of Formula I has M=Hf     -   X is a sigma ligand     -   R are the same or different from each other and can be saturated         linear or branched C₁-C₁₀ alkyl, C₅-C₁₀ aryl, C₆-C₂₀ alkylaryl         or C₆-C₂₀ arylalkyl groups, which can optionally contain up to 2         heteroatoms or silicon atoms     -   R¹ is a C₆-C₂₀-aryl, which can be unsubstituted or substituted         by one or up to 5 linear or branched C₁-C₁₀ alkyl group(s)     -   R² is a saturated linear or cyclic C₃-C₂₀ alkyl group or a         branched CR³R⁴R⁵ group, wherein R³ is hydrogen or an C₁-C₂₀         alkyl group and R⁴ and R⁵ are the same or are different and can         be an C₁-C₂₀ alkyl group.     -   and     -   (ii) a boron containing cocatalyst

Viewed from another aspect the invention provides a process for the preparation of an ethylene copolymer comprising polymerizing ethylene and a C₄₋₁₀ alpha-olefin comonomer in a high temperature solution process at a temperature greater than 100° C. in the presence of a catalyst comprising:

-   -   (i) a metallocene complex of formula (I) as defined above and     -   (ii) a boron containing cocatalyst.

Viewed from a further aspect the invention provides an ethylene copolymer made by a process as hereinbefore defined.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 . Productivity (kg-PO/g-MC) vs. cocatalyst and vs metallocenes.

FIG. 2 . Mw (kDa) vs. cocatalyst and vs metallocenes.

FIG. 3 . C8 in polymer (wt %) vs. cocatalyst and vs metallocenes.

DETAILED DESCRIPTION OF THE INVENTION

Metallocene Complex

The single site metallocene complex, especially the complexes defined by the formula (I) specified in the present invention, used for manufacture of the ethylene copolymer are asymmetrical, meaning that the two ligands forming the metallocene complex are different.

The invention can be effected with a metallocene complex of formula (I)

wherein

-   -   M is Hf or a mixture with Zr, provided that more than 50% by         moles of the complex of Formula I has M=Hf     -   X is a sigma ligand     -   R are the same or different from each other and can be saturated         linear or branched C₁-C₁₀ alkyl, C₅-C₁₀ aryl, C₆-C₂₀ alkylaryl         or C₆-C₂₀ arylalkyl groups, which can optionally contain up to 2         heteroatoms or silicon atoms     -   R¹ is a C₆-C₂₀-aryl, which can be unsubstituted or substituted         by one or up to 5 linear or branched C₁-C₁₀ alkyl group(s)     -   R² is a saturated linear or cyclic C₃-C₂₀ alkyl group or a         branched CR³R⁴R⁵ group, wherein R³ is hydrogen or a C₁-C₂₀ alkyl         group and R⁴ and R⁵ are the same or are different and can be an         C₁-C₂₀ alkyl group.

In the formula (I) each X, which may be the same or different, is a sigma ligand, preferably a hydrogen atom, a halogen atom, a R⁶, OR⁶, OSO₂CF₃, OCOR⁶, SR⁶, NR⁶ ₂ or PR⁶ ₂ group wherein R⁶ is a linear or branched, cyclic or acyclic, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₆-C₂₀-aryl, C₇-C₂₀-alkylaryl or C₇-C₂₀-arylalkyl radical; optionally containing heteroatoms belonging to groups 14-16 or is SiR⁶ ₃, SiHR⁶ ₂ or SiH₂R⁶. R⁶ is preferably C₁₋₆ alkyl, phenyl or benzyl group.

The term halogen includes fluoro, chloro, bromo and iodo groups, preferably chloro groups.

More preferably each X is independently a halogen atom or a R⁶ or OR⁶ group, whereby R⁶ is a C₁₋₆-alkyl, phenyl or benzyl group.

Most preferably X is methyl, chloro or benzyl group. Preferably both X groups are the same.

M is preferably Hf.

R are the same or different from each other and can be saturated linear or branched C₁-C₁₀ alkyl, C₅-C₁₀ aryl, C₆-C₂₀ alkylaryl or C₆-C₂₀ arylalkyl groups, which can optionally contain up to 2 heteroatoms or silicon atoms.

C₆-C₂₀ alkylaryl group is meant to be an C₆-C₁₀ aryl group which is substituted by one or more alkyl groups which may be the same or different, whereby the number of C-atoms in the alkyl group substituents is in a range which leads to C₆-C₂₀ alkylaryl groups.

Preferably R are the same or different from each other and can be saturated linear or branched C₁-C₆ alkyl, C₆-C₁₀ aryl, C₆-C₂₀ alkylaryl or C₆-C₂₀ arylalkyl groups, which do not contain heteroatoms or silicon atoms.

More preferably all R are the same and are saturated linear or branched C₁-C₆ alkyl or C₆-C₁₀ aryl, and even more preferred all R are the same and are a saturated linear or branched C₁-C₆ alkyl.

Most preferably all R are the same and are all C₁ alkyl groups.

R¹ is a C₆-C₂₀-aryl group, which can be unsubstituted or substituted by one or up to 5 linear or branched C₁-C₁₀ alkyl group(s).

Preferably R¹ is a C₆-C₁₀-aryl group which can be unsubstituted or substituted by one linear or branched C₁-C₆ alkyl group.

More preferably R¹ is an unsubstituted C₆-C₁₀-aryl group, most preferably R¹ is phenyl.

R² is a saturated linear or cyclic C₃-C₂₀ alkyl group or a branched CR³R⁴R⁵ group, wherein R³ is hydrogen or an C₁-C₂₀ alkyl group, preferably hydrogen and R⁴ and R⁵ are the same or are different and can be an C₁-C₂₀ alkyl group.

Preferably R² is a saturated linear or cyclic C₃-C₁₀ alkyl group or a branched CR³R⁴R⁵ group, wherein R³ is hydrogen and R⁴ and R⁵ are the same or are different and can be an C₁-C₁₀ alkyl group.

More preferably R² is a saturated linear or cyclic C₅-C₁₀ alkyl group or a branched CR³R⁴R⁵ group, wherein R³ is hydrogen and R⁴ and R⁵ are the same or are different and can be an C₁-C₃ alkyl group.

Most preferably R² is i-propyl, n-hexyl or cyclohexyl.

Especially preferred complexes of formula (I) are

-   (Phenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dibenzyl -   (Phenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dimethyl -   (Phenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dibenzyl -   (Phenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dimethyl -   (Phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butyfluoren-9-yl)hafnium     dibenzyl -   (Phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butyfluoren-9-yl)hafnium     dimethyl -   (Phenyl)(cyclopentyl)methylene(cyclopentadienyl)(2,7-di-tert-butyfluoren-9-yl)hafnium     dibenzyl -   (Phenyl)(cyclopentyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dimethyl -   (para-isopropylphenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butyfluoren-9-yl)hafnium     dibenzyl -   (para-isopropylphenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butyfluoren-9-yl)hafnium     dimethyl -   (para-isopropylphenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dibenzyl -   (para-isopropylphenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dimethyl -   (para-isopropylphenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dibenzyl -   (para-isopropylphenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dimethyl -   (para-isopropylphenyl)(cyclopentyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dibenzyl -   (para-isopropyl)(cyclopentyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium     dimethyl

Even more preferred are the dimethyl-complexes.

Cocatalyst

To form an active catalytic species it is normally necessary to employ a cocatalyst as is well known in the art. The present invention requires the use of a boron containing cocatalyst.

Boron based cocatalysts of interest include boron compounds containing a borate 3⁺ ion, i.e. borate compounds. These compounds generally contain an anion of formula: (Z)₄ B ⁻  (II)

where Z is an optionally substituted phenyl derivative, said substituent being a halo-C₁₋₆-alkyl or halo group. Preferred options are fluoro or trifluoromethyl. Most preferably, the phenyl group is perfluorinated.

Such ionic cocatalysts preferably contain a non-coordinating anion such as tetrakis(pentafluorophenyl)borate.

Suitable counterions are protonated amine or aniline derivatives or phosphonium ions. These may have the general formula (III) or (IV): NQ₄ ⁺(III) or PQ₄ ⁺  (IV)

where Q is independently H, C₁₋₆-alkyl, C₃₋₈ cycloalkyl, phenylC₁₋₆-alkylene- or optionally substituted Ph. Optional substituents may be C1-6-alkyl, halo or nitro. There may be one or more than one such substituent. Preferred substituted Ph groups include therefore para-substituted phenyl, preferably tolyl or dimethylphenyl.

It is preferred if at least one Q group is H, thus preferred compounds are those of formula: NHQ₃ ⁺(V) or PHQ₃ ⁺  (VI)

Preferred phenylC₁₋₆-alkyl-groups include benzyl.

Suitable counterions therefore include: methylammonium, anilinium, dimethylammonium, diethylammonium, N-methylanilinium, diphenylammonium, N,N-dimethylanilinium, trimethylammonium, triethylammonium, tri-n-butylammonium, methyldiphenylammonium, p-bromo-N,N-dimethylanilinium or p-nitro-N,N-dimethylanilinium, especially dimethylammonium or N,N-dimethylanilinium. The use of pyridinium as an ion is a further option.

Phosphonium ions of interest include triphenylphosphonium, triethylphosphonium, diphenylphosphonium, tri(methylphenyl)phosphonium and tri(dimethylphenyl)phosphonium. A more preferred counterion is trityl (CPh₃ ⁺) or analogues thereof in which the Ph group is functionalised to carry one or more alkyl groups. Highly preferred borates of use in the invention therefore comprise the tetrakis(pentafluorophenyl)borate ion.

Preferred ionic compounds which can be used according to the present invention include:

-   tributylammoniumtetra(pentafluorophenyl)borate, -   tributylammoniumtetra(trifluoromethylphenyl)borate, -   tributylammoniumtetra-(4-fluorophenyl)borate, -   N,N-dimethylcyclohexylammoniumtetrakis-(pentafluorophenyl)borate, -   N,N-dimethylbenzylammoniumtetrakis(pentafluorophenyl)borate, -   N, N-dimethylaniliniumtetrakis(pentafluorophenyl)borate, -   N,N-di(propyl)ammoniumtetrakis(pentafluorophenyl)borate, -   di(cyclohexyl)ammoniumtetrakis(pentafluorophenyl)borate, -   triphenylcarbeniumtetrakis(pentafluorophenyl)borate, -   ferroceniumtetrakis(pentafluorophenyl)borate.

Preference is given to triphenylcarbeniumtetrakis(pentafluorophenyl) borate,

-   N,N-dimethylcyclohexylammoniumtetrakis(pentafluorophenyl)borate, -   N,N-dimethylbenzylammoniumtetrakis(pentafluorophenyl)borate or -   N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate.

More preferred borates are triphenylcarbeniumtetrakis(pentafluorophenyl) borate and N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate. N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate is most preferred.

It is further possible to add an aluminium alkyl compound. Suitable aluminium alkyl compounds are compounds of the formula (VIII) AIR₃ with R being a linear or branched C₂-C₈-alkyl group. Preferred aluminium alkyl compounds are triethylaluminium, tri-isobutylaluminium, tri-isohexylaluminium, tri-n-octylaluminium and tri-isooctylaluminium.

Suitable amounts of cocatalyst will be well known to the skilled man.

The molar ratio of boron to the metal ion of the metallocene may be in the range 0.5:1 to 10:1 mol/mol, preferably 1:1 to 10:1, especially 1:1 to 5:1 mol/mol.

Even more preferred is a molar ratio of boron to the metal ion of the metallocene from 1:1 to less than 2:1 mol/mol, e.g from 1:1 to 1.8:1 or 1:1 to 1.5:1.

Catalyst Manufacture

The metallocene complex of the present invention is used in combination with the cocatalyst(s) as a catalyst system for the polymerization of ethylene and C₄₋₁₀ alpha-olefin comonomer in a high temperature solution polymerization process.

The catalyst system of the invention may be used as a homogeneous catalyst or heterogeneous catalyst, preferably as homogeneous catalyst system.

Homogeneous or non-supported catalyst systems, suitable for the present invention can be prepared in solution, for example in an hydrocarbon solvent like hexane, cyclohexane, heptane, light naphta or toluene, by contacting the metallocene (as a solid or as a solution) with the cocatalyst(s), for example a borane or a borate salt as slurry in a hydrocarbon diluent or previously dissolved in an aromatic solvent, or preferably can be formed by sequentially adding the catalyst components directly into the polymerization reactor.

Polymer

The polymer to be produced using the catalyst system of the invention is copolymer of ethylene and a C₄₋₁₀ alpha-olefin comonomer, like 1-butene, 1-hexene, 4-methyl-1-pentene, 1-octene etc. Preferably butene, hexene or octene and more preferably octene is used as comonomer. The comonomer content in such a polymer may be up to 45 mol %, preferably between 1 to 40 mol %, more preferably 1.5 to 35 mol % and even more preferably 2 to 25 mol %.

The density (measured according to ISO 1183-187) of the polymers is in the range of 0.850 g/cm³ to 0.930 g/cm³, preferably in the range of 0.850 g/cm³ to 0.920 g/cm³ and more preferably in the range of 0.850 g/cm³ to 0.910 g/cm³.

Mw/Mn value of the polymers of the invention is less than 5, e.g. in the range of 2.0 to 4.5.

The melting points (measured with DSC according to ISO 11357-3:1999) of the polymers to be produced are below 130° C., preferably below 120° C., more preferably below 110° C. and most preferably below 100° C.

Polymerization

The catalyst system of the present invention is used to produce the above defined ethylene copolymers in a high temperature solution polymerization process at temperatures higher than 100° C.

In view of this invention such process is essentially based on polymerizing the monomer and a suitable comonomer in a liquid hydrocarbon solvent in which the resulting polymer is soluble. The polymerization is carried out at a temperature above the melting point of the polymer, as a result of which a polymer solution is obtained. This solution is flashed in order to separate the polymer from the unreacted monomer and the solvent. The solvent is then recovered and recycled in the process.

A solution polymerization process is known for its short reactor residence times (compared to Gas-phase or slurry processes) allowing, thus, very fast grade transitions and significant flexibility in producing a wide product range in a short production cycle.

According to the present invention the used solution polymerization process is a high temperature solution polymerization process, using a polymerization temperature of higher than 100° C. Preferably the polymerization temperature is at least 110° C., more preferably at least 150° C. The polymerization temperature can be up to 250° C.

The pressure in the used solution polymerization process according to the invention is preferably in a range of 10 to 100 bar, preferably 15 to 100 bar and more preferably 20 to 100 bar.

The liquid hydrocarbon solvent used is preferably a C₅₋₁₂-hydrocarbon which may be unsubstituted or substituted by C₁₋₄ alkyl group such as pentane, methyl pentane, hexane, heptane, octane, cyclohexane, methylcyclohexane and hydrogenated naphtha. More preferably unsubstituted C₆₋₁₀-hydrocarbon solvents are used.

Advantage

The new catalyst systems, comprising component (i) and (ii) can be advantageously used for ethylene copolymerization in high temperature solution polymerization process.

The catalyst systems according to the present invention show improved balance of solubility, productivity, comonomer incorporation ability and molecular weight capability, if used for ethylene copolymerization in high temperature solution polymerization process.

Applications

The polymers made by the catalyst system of the invention are useful in all kinds of end articles such as pipes, films (cast or blown films), fibers, moulded articles (e.g. injection moulded, blow moulded, rotomoulded articles), extrusion coatings and so on.

The invention will now be illustrated by reference to the following non-limiting examples

EXAMPLES

Methods

DSC

Temperature modulated DSC experiments were performed in a TA Instruments Q2000 DSC operated in modulated mode and calibrated with indium, tin and zinc according to ISO 11357-1. Circa 5 mg of the sample were placed in an aluminium pan. The temperature was initially raised to 180° C. and afterwards lowered to −88° C. at 10° C./min as in standard DSC. Afterwards the temperature was raised by a temperature modulated scan with heating rate of 2° C./min modulated of 0.32° C. every 60 seconds. The glass transition temperature was measured from the reversible heat flow thermogram as the inversion point at transition.

If the polymer composition has been estimated by Tg(DSC) the following internal correlation has been used: C8(wt %)=(Tg(° C.)+19.16)/−1.059

Zr and Hf Determination (ICP-Method)

The elementary analysis of a catalyst was performed by taking a solid sample of mass, M, cooling over dry ice. Samples were diluted up to a known volume, V, by dissolving in nitric acid (HNO₃, 65%, 5% of V) and freshly deionised (DI) water (5% of V). The solution was then added to hydrofluoric acid (HF, 40%, 3% of V), diluted with DI water up to the final volume, V, and left to stabilise for two hours.

The analysis was run at room temperature using a Thermo Elemental iCAP 6300 Inductively Coupled Plasma—Optical Emission Spectrometer (ICP-OES) which was calibrated using a blank (a solution of 5% HNO₃, 3% HF in DI water), and 6 standards of 0.5 ppm, 1 ppm, 10 ppm, 50 ppm, 100 ppm and 300 ppm of Al, with 0.5 ppm, 1 ppm, 5 ppm, 20 ppm, 50 ppm and 100 ppm of Hf and Zr in solutions of 5% HNO3, 3% HF in DI water.

Immediately before analysis the calibration is ‘resloped’ using the blank and 100 ppm Al, 50 ppm Hf, Zr standard, a quality control sample (20 ppm Al, 5 ppm Hf, Zr in a solution of 5% HNO3, 3% HF in DI water) is run to confirm the reslope. The QC sample is also run after every 5th sample and at the end of a scheduled analysis set.

The content of hafnium was monitored using the 282.022 nm and 339.980 nm lines and the content for zirconium using 339.198 nm line. The content of aluminium was monitored via the 167.079 nm line, when Al concentration in ICP sample was between 0-10 ppm (calibrated only to 100 ppm) and via the 396.152 nm line for Al concentrations above 10 ppm.

The reported values are an average of three successive aliquots taken from the same sample and are related back to the original catalyst by inputting the original mass of sample and the dilution volume into the software.

Quantification of Comonomer Content by NMR Spectroscopy

Quantitative nuclear-magnetic resonance (NMR) spectroscopy was used to quantify the comonomer content of the polymers.

Quantitative ¹³C{¹H} NMR spectra recorded in the molten-state using a Bruker Advance III 500 NMR spectrometer operating at 500.13 and 125.76 MHz for ¹H and ¹³C respectively. All spectra were recorded using a ¹³C optimised 7 mm magic-angle spinning (MAS) probe-head at 150° C. using nitrogen gas for all pneumatics. Approximately 200 mg of material was packed into a 7 mm outer diameter zirconia MAS rotor and spun at 4 kHz. This setup was chosen primarily for the high sensitivity needed for rapid identification and accurate quantiflcation.^([1], [2], [3], [4]) Standard single-pulse excitation was employed utilising the transient NOE at short recycle delays of 3s^([5], [1]) and the RS-HEPT decoupling scheme.^([6], [7]) A total of 1024 (1 k) transients were acquired per spectrum. This setup was chosen due to its high sensitivity towards low comonomer contents.

Quantitative ¹³C{¹H} NMR spectra were processed, integrated and quantitative properties determined using custom spectral analysis automation programs. All chemical shifts are internally referenced to the bulk methylene signal (δ+) at 30.00 ppm.^([8])

Characteristic signals corresponding to the incorporation of 1-octene were observed^([8], [9], [10], [11], [12]) and all comonomer contents calculated with respect to all other monomers present in the polymer.

Characteristic signals resulting from isolated 1-octene incorporation i.e. EEOEE comonomer sequences, were observed. Isolated 1-octene incorporation was quantified using the integral of the signal at 38.32 ppm. This integral is assigned to the unresolved signals corresponding to both _(*)B6 and _(*)βB6B6 sites of isolated (EEOEE) and isolated double non-consecutive (EEOEOEE) 1-octene sequences respectively. To compensate for the influence of the two _(*)βB6B6 sites the integral of the ββB6B6 site at 24.7 ppm is used: O=I _(*B6+) _(*) _(βB6B6)−2*I _(ββB6B6)

Characteristic signals resulting from consecutive 1-octene incorporation, i.e. EEOOEE comonomer sequences, were also observed. Such consecutive 1-octene incorporation was quantified using the integral of the signal at 40.48 ppm assigned to the ααB6B6 sites accounting for the number of reporting sites per comonomer: OO=2*I _(ααB6B6)

Characteristic signals resulting from isolated non-consecutive 1-octene incorporation, i.e. EEOEOEE comonomer sequences, were also observed. Such isolated non-consecutive 1-octene incorporation was quantified using the integral of the signal at 24.7 ppm assigned to the ββB6B6 sites accounting for the number of reporting sites per comonomer. OEO=2*I _(ββB6B6)

Characteristic signals resulting from isolated triple-consecutive 1-octene incorporation, i.e. EEOOOEE comonomer sequences, were also observed. Such isolated triple-consecutive 1-octene incorporation was quantified using the integral of the signal at 41.2 ppm assigned to the ααγB6B6B6 sites accounting for the number of reporting sites per comonomer: OOO=3/2 *I _(ααγB6B6B6)

With no other signals indicative of other comonomer sequences observed the total 1-octene comonomer content was calculated based solely on the amount of isolated (EEOEE), isolated double-consecutive (EEOOEE), isolated non-consecutive (EEOEOEE) and isolated triple-consecutive (EEOOOEE) 1-octene comonomer sequences: O _(total) =O+OO+OEO+OOO

Characteristic signals resulting from saturated end-groups were observed. Such saturated end-groups were quantified using the average integral of the two resolved signals at 22.84 and 32.23 ppm. The 22.84 ppm integral is assigned to the unresolved signals corresponding to both 2B6 and 2S sites of 1-octene and the saturated chain end respectively. The 32.23 ppm integral is assigned to the unresolved signals corresponding to both 3B6 and 3S sites of 1-octene and the saturated chain end respectively. To compensate for the influence of the 2B6 and 3B6 1-octene sites the total 1-octene content is used: S=(½)*(I _(2S°2B6) +I _(3S+3B6)−2*O _(total))

The ethylene comonomer content was quantified using the integral of the bulk methylene (bulk) signals at 30.00 ppm. This integral included the γ and 4B6 sites from 1-octene as well as the δ⁺ sites. The total ethylene comonomer content was calculated based on the bulk integral and compensating for the observed 1-octene sequences and end-groups: E _(total)=(½)*[I _(bulk)+2*O+1*OO+3*OEO+0*OOO+3*S]

It should be noted that compensation of the bulk integral for the presence of isolated triple-incorporation (EEOOOEE) 1-octene sequences is not required as the number of under and over accounted ethylene units is equal.

The total mole fraction of 1-octene in the polymer was then calculated as: fO=(O _(total)/(E _(total) +O _(total))

The total comonomer incorporation of 1-octene in weight percent was calculated from the mole fraction in the standard manner O[wt %]=100*(fO*112.21)/((fO*112.21)+((1-fO)*28.05))

-   [1] Klimke, K., Parkinson, M., Piel, C., Kaminsky, W., Spiess, H.     W., Wilhelm, M., Macromol. Chem. Phys. 2006; 207:382. -   [2] Parkinson, M., Klimke, K., Spiess, H. W., Wilhelm, M., Macromol.     Chem. Phys. 2007; 208:2128. -   [3] Castignolles, P., Graf, R., Parkinson, M., Wilhelm, M.,     Gaborieau, M., Polymer 50 (2009) 2373 -   [4] NMR Spectroscopy of Polymers: Innovative Strategies for Complex     Macromolecules, Chapter 24, 401 (2011) -   [5] Pollard, M., Klimke, K., Graf, R., Spiess, H. W., Wilhelm, M.,     Sperber, O., Piel, C., Kaminsky, W., Macromolecules 2004; 37:813. -   [6] Filip, X., Tripon, C., Filip, C., J. Mag. Resn. 2005, 176, 239 -   [7] Griffin, J. M., Tripon, C., Samoson, A., Filip, C., and     Brown, S. P., Mag. Res. in Chem. 2007 45, S1, S198 -   [8] J. Randall, Macromol. Sci., Rev. Macromol. Chem. Phys. 1989,     C29, 201. [9] Liu, W., Rinaldi, P., McIntosh, L., Quirk, P.,     Macromolecules 2001, 34, 4757 -   [10] Qiu, X., Redwine, D., Gobbi, G., Nuamthanom, A., Rinaldi, P.,     Macromolecules 2007, 40, 6879 -   [11] Busico, V., Carbonniere, P., Cipullo, R., Pellecchia, R.,     Severn, J., Talarico, G., Macromol. Rapid Commun. 2007, 28, 1128 -   [12] Zhou, Z., Kuemmerle, R., Qiu, X., Redwine, D., Cong, R., Taha,     A., Baugh, D. Winniford, B., J. Mag. Reson. 187 (2007) 225

GPC: Molecular weight averages, molecular weight distribution, and polydispersity index (M_(n), M_(w), M_(w)/M_(n)) Molecular weight averages (Mw, Mn), Molecular weight distribution (MWD) and its broadness, described by polydispersity index, PDI=Mw/Mn (wherein Mn is the number average molecular weight and Mw is the weight average molecular weight) of the polymer were determined by high temperature size exclusion chromatography (HT-SEC) on a Polymer Laboratories PLXT-20 Rapid GPC Polymer Analysis System (including pump, refractive index detector and viscosity detector) at 160° C. with 3 PLgel Olexis (300×7.5 mm, Polymer Laboratories) columns in series. 1,2,4-Trichlorobenzene containing butylated hydroxytoluene (0.5 g/L) and Irganox 1010 (20 mg/L) was used as eluent at a flow rate of 1.0 mL/min. The molecular weights were calculated with respect to polyethylene standards (Polymer Laboratories, Mp=5.310 up to Mp=1.510.000 g/mol). A Polymer Laboratories PL XT-220 robotic sample handling system was used as autosampler. The concentration of the samples was between 2 and 4 mg polymer/mL of TCB.

Determination of the Relative Comonomer Reactivity Ratio R

Ethylene concentration in liquid phase can be considered constant since total pressure is kept constant by feeding ethylene during polymerization. The C₈/C₂ ratio in solution at the end of the polymerization is calculated by subtracting the amount of octene incorporated in the polymer from the measured composition of the latter (% wt 1-octene)

The reactivity ratio, R, for each catalyst is then calculated as: R=[(C ₈ /C ₂)_(pol)]/[(C ₈ /C ₂)_(average in liquid phase)]

where (C₈/C₂)_(average in liquid phase) is calculated as ((C₈/C₂)_(final)+(C₈/C₂)_(feed))/2

Solubility of the Hafnium Complex in Hexane

Procedure for the Solubility Test:

All experiments were carried out under inert atmosphere in a septum bottle.

-   -   1. Inside the glovebox, 10.5 mg of complex was weighted in a         septum bottle.     -   2. 1 g of hexane was added to the solid complex     -   3. After stirring for 20 h at room temperature, solution is         checked     -   4. if no insoluble material is observed, repeat steps 1 and 3         until you reach saturation and insoluble materials are observed.

Chemicals

MAO was purchased from Chemtura and used as a 30 wt-% solution in toluene.

Triphenylcarbeniumtetrakis(pentafluorophenyl)borate (TB) (alternative name trityl tetrakis-(pentafluorophenyl)borate) (CAS 136040-19-2) was purchased from Acros (tritylBF20)

N,N-Dimethylanilinium Tetrakis(pentafluorophenyl)borate (AB) (CAS 118612-00-3) was purchased from Boulder.

1-octene as co-monomer (99%, Sigma Aldrich) was dried over molecular sieves and degassed with nitrogen before use.

Heptane and decane (99.9%, Sigma Aldrich) were dried under molecular sieves and degassed with nitrogen before use.

Catalyst Preparation Examples

a) Complex Preparation:

Complex-C0

[1-(η⁵-Cyclopentadien-1-yl)-1-(η⁵-2,7-di-tert-butylfluorenyl)-1,1-diphenylmethane]hafnium dimethyl

Diphenylmethylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium diclorde was synthesized according to the literature Hopf, A, Kaminsky, W., Catalysis Communications 2002; 3:459.

To a solution of 3.78 g (5.0 mmol) of [1-(η⁵-cyclopentadien-1-yl)-1-(η⁵-2,7-di-tert-butylfluorenyl)-1,1-diphenylmethane]hafnium dichloride in a mixture of 50 ml of toluene and 50 mi of ether 7.0 ml (14.77 mmol) of 2.11 M MeMgBr in ether was added. The resulting mixture was refluxed for 30 min and then evaporated to ca. 25 ml. The obtained mixture was heated to 80-90° C. and filtered while hot through glass frit (G4) to remove insoluble magnesium salts. The filter cake was additionally washed with 5×20 ml of warm hexane. The combined filtrate was evaporated to ca. 5 ml, and then 20 ml of hexane was added to the residue. Yellow powder precipitated from this solution was collected and dried in vacuum. This procedure gave 3.14 g (88%) of pure [1-(η⁵-cyclopentadien-1-yl)-1-(η⁵-2,7-di-tert-butylfluorenyl)-1,1-diphenylmethane]hafnium dimethyl.

Anal. calc. for C₄₁H₄₄Hf C, 68.85; H, 6.20. Found: C, 69.10; H, 6.37.

¹H NMR (CDCl₃): δ 8.07 (d, J=8.9 Hz, 2H), 7.95 (br.d, J=7.9 Hz, 2H), 7.85 (br.d, J=7.9 Hz, 2H), 7.44 (dd, J=8.9 Hz, J=1.5 Hz, 2H), 7.37 (td, J=7.6 Hz, J=1.2 Hz, 2H), 7.28 (td, J=7.6 Hz, J=1.2 Hz, 2H), 7.24-7.17 (m, 2H), 6.26 (s, 2H), 6.20 (t, J=2.7 Hz, 2H), 5.45 (t, J=2.7 Hz, 2H), 1.03 (s, 18H), −1.90 (s, 6H). ¹³C{¹H} NMR (CDCl₃,): δ 148.46, 145.75, 129.69, 128.63, 128.46, 126.73, 126.54, 123.29, 122.62, 120.97, 118.79, 116.09, 111.68, 107.76, 101.56, 76.47, 57.91, 37.61, 34.88, 30.84.

Complex 1 (C1):

(Phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butyfluoren-9-yl)hafnium dimethyl Step 1: 6-Phenyl-6-hexylfulvene

To a solution of 23.8 g (125.1 mmol) of 1-phenylheptan-1-one in 50 ml of THF cooled in an ice-bath, a solution of 25.4 g (150 mmol, 1.2 equiv.) of cyclopentadienylmagnesium bromide in 150 ml of THF was added dropwise. The resulting mixture was refluxed for 3 h, then stirred overnight at room temperature, then cooled in an ice-bath and then quenched with 10% HCl to pH˜5-6. This mixture was extracted with 3×150 ml of hexane; the combined organic extract was dried over Na₂SO₄ and then evaporated to dryness to give a dark-red oil. The product was isolated by flash-chromatography on silica gel 60 (40-63 μm; eluent: hexane-ethyl acetate=100:1, vol.). This procedure gave 14.25 g (48%) of 6-phenyl-6-hexylfulvene as reddish oil.

Anal. calc. for C₁₈H₂₂: C, 90.70; H, 9.30. Found: C, 90.87; H, 9.27.

¹H NMR (CDCl₃): δ 7.37-7.30 (m, 5H), 6.63 (ddd, J=5.3 Hz, J=2.0 Hz, J=1.5 Hz, 1H), 6.55 (ddd, J=5.3 Hz, J=2.0 Hz, J=1.5 Hz, 1H), 6.46 (ddd, J=5.3 Hz, J=2.0 Hz, J=1.5 Hz, 1H), 6.10 (ddd, J=5.3 Hz, J=2.0 Hz, J=1.5 Hz, 1H), 2.90 (t, J=7.6 Hz, 2H), 1.47-1.36 (m, 2H), 1.34-1.15 (m, 6H), 0.83 (t, J=6.9 Hz, 3H). ¹³C{¹H} NMR (CDCl₃): δ 154.81, 143.31, 140.87, 131.71, 131.32, 129.42, 127.97, 127.73, 123.86, 120.90, 36.25, 31.51, 29.54, 29.13, 22.46, 13.97.

Step 2: (Phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfiuoren-9-yl)hafnium dichloride

To a solution of 14.88 g (53.44 mmol) of 2,7-di-tert-butylfluorene in 200 ml of THF cooled to −50° C. 21.4 ml (53.5 mmol) of 2.5 M ^(n)BuLi in hexanes was added in one portion. This mixture was stirred overnight at room temperature. The resulting reddish solution was cooled to −50° C., and a solution of 14.25 g (59.78 mmol) of 6-phenyl-6-hexylfulvene in 200 ml of THF was added in one portion. After stirring overnight at room temperature the dark-red reaction mixture was cooled in an ice-bath and then quenched with a solution of 5 ml of 12 M HCl in 200 ml of water. The resulting yellow mixture was extracted with 400 ml of dichloromethane. The organic layer was separated, and the aqueous one was extracted with 150 ml of dichloromethane. The combined organic extract was dried over Na₂SO₄ and filtered through a pad of silica gel 60 (40-63 μm) which was additionally washed by 2×50 ml of dichloromethane. The combined filtrate was evaporated to dryness to give 29.1 g of phenyl-(1-hexyl)-cyclopentadienyl-(2,7-di-tert-butylfluoren-9-yl)methane which was used without further purification. To a solution of 16.2 g (31.35 mmol) of phenyl-(1-hexyl)-cyclopentadienyl-(2,7-di-tert-butylfluorenyl)methane (as prepared above) in 250 ml of ether cooled to −78° C., 25.0 ml (62.5 mmol) of 2.5 M ^(n)BuLi in hexanes was added in one portion. The formed mixture was stirred overnight at room temperature and then cooled to −50° C., and 10.04 g (31.35 mmol) of HfCl₄ was added. The obtained mixture was stirred for 24 h at room temperature and then evaporated to dryness. The residue was stirred with 200 ml of warm toluene, and the formed suspension was filtered through a glass frit (G4). The filtrate was evaporated to ca. 40 ml. Yellow crystalline material precipitated from this mixture over a week at −30° C. was separated, washed with 3×15 ml of a mixture of toluene and hexane (1:3, vol.) and dried in vacuum. This procedure gave 14.2 g (59%) of (phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butyfluoren-9-yl)-]hafnium dichloride.

Anal. calc. for C₃₉H₄₆Cl₂Hf: C, 61.30; H, 6.07. Found: C, 61.53; H, 6.26.

¹H NMR (CDCl₃): δ 8.01 (d, J=8.9 Hz, 1H), 7.95 (d, J=8.9 Hz, 1H), 7.82 (dm, J=7.9 Hz, 1H), 7.70 (s, 1H), 7.66-7.58 (m, 2H), 7.58-7.52 (m, 1H), 7.52-7.46 (m, 1H), 7.44-7.36 (m, 2H), 6.36-6.30 (m, 1H), 6.23-6.17 (m, 1H), 6.13 (s, 1H), 5.80-5.74 (m, 1H), 5.55-5.49 (m, 1H), 3.13-2.97 (m, 1H), 2.80-2.65 (m, 1H), 1.64-1.44 (m, 3H), 1.40 (s, 9H), 1.36-1.18 (m, 5H), 0.99 (s, 9H), 0.85 (t, J=7.9 Hz, 3H). ¹³C{¹H} NMR (CDCl₃,): 6152.11, 149.53, 143.32, 130.53, 128.46, 128.26, 127.17, 127.05, 124.17, 124.14, 123.97, 123.49, 122.63, 120.25, 119.84, 119.65, 118.84, 118.79, 117.87, 116.58, 114.58, 99.64 (two resonances), 77.83, 53.68, 41.28, 35.42, 34.84, 31.88, 31.11, 30.51, 29.75, 24.03, 22.63, 14.05.

Step 3: (Phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl

To a solution of 3.82 g (5.0 mmol) of (phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dichloride in a mixture of 50 ml of toluene and 50 ml of ether 7.0 ml (14.77 mmol) of 2.11 M MeMgBr in ether was added. The resulting mixture was refluxed for 30 min and then evaporated to ca. 25 ml. The obtained solution was heated to 80-90° C. and filtered while hot through glass frit (G3) to remove insoluble magnesium salts. The filter cake was additionally washed with 2×20 ml of toluene. The combined filtrate was evaporated to dryness, and 20 ml of hexane was added to the residue. The resulting suspension was filtered once again through a glass frit (G4). The filtrate was evaporated to dryness, and the residue was dissolved in 7 ml of hexane. Yellow powder precipitated from this solution overnight at −40° C. was collected and dried in vacuum. This procedure gave 2.55 g (71%) of pure (phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl.

Anal. calc. for C₄₁H₅₂Hf: C, 68.08; H, 7.25. Found: C, 68.11; H, 7.46.

¹H NMR (CDCl₃): δ 8.07 (d, J=8.9 Hz, 1H), 7.98 (d, J=8.9 Hz, 1H), 7.81 (dm, J=7.9 Hz, 1H), 7.63-7.56 (m, 2H), 7.53-7.43 (m, 2H), 7.38-7.30 (m, 3H), 6.28-6.21 (m, 1H), 6.14-6.08 (m, 1H), 6.03 (s, 1H), 5.65-5.59 (m, 1H), 5.34-5.28 (m, 1H), 2.92-2.81 (m, 1H), 2.59-2.48 (m, 1H), 1.52-1.40 (m, 3H), 1.38 (s, 9H), 1.34-1.17 (m, 5H), 0.97 (s, 9H), 0.84 (t, J=7.0 Hz, 3H), −1.76 (s, 3H), −1.90 (s, 3H). ¹³C{¹H} NMR (CDCl₃,): δ 150.18, 147.73, 144.31, 130.72, 128.04, 127.90, 127.20, 126.59, 124.49, 123.74, 122.90, 122.73, 121.01, 120.61, 119.11, 117.56, 116.32, 115.83, 112.85, 111.08, 109.58, 100.94, 100.57, 76.51, 53.50, 41.19, 38.16, 37.39, 35.32, 34.75, 31.93, 31.35, 30.75, 29.86, 24.12, 22.68, 14.08.

Complex 2 (C2):

(Phenyl)cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl Step 1: 6-Phenyl-6-cyclohexylfulvene

To a solution of sodium ethoxide obtained from 6.11 g (267.7 mmol) of sodium metal and 160 ml of dry ethanol 22.0 g (332.8 mmol) of cyclopentadiene was added dropwise over 10 min and the resulting red solution was stirred 0.5 h at room temperature. Then, 25.0 g (132.8 mmol) of phenyl cyclohexyl ketone was added and the resulting dark-red mixture was stirred 22 h at room temperature. Then, it was poured into 1000 ml of water. After acidification with 2 M HCl to pH ca. 6.5, the product was extracted with 500 ml of dichloromethane. The organic layer was separated, dried over Na₂SO₄ and concentrated under a reduced pressure. The product was isolated by flash-chromatography on silica gel 60 (40-63 um, 800 ml; eluent: hexane). This procedure gave 22.09 g (70%) of 6-phenyl-6-cyclohexylfulvene as a light-red oil which completely solidified upon storage at −30° C.

Anal. calc. for C₁₈H₂₀: C, 91.47; H, 8.53. Found: C, 91.79; H, 8.72.

¹H NMR (CDCl₃): δ 7.35-7.29 (m, 3H), 7.19-7.14 (m, 2H), 6.71 (dt, J=5.4 Hz, J=1.6 Hz, 1H), 6.54 (dt, J=5.4 Hz, J=1.6 Hz, 1H), 6.36 (dt, J=5.3 Hz, J=1.5 Hz, 1H), 5.74 (dt, J=5.3 Hz, J=1.7 Hz, 1H), 3.10 (tt, J=11.8 Hz, J=3.2 Hz, 1H), 1.85-1.73 (m, 4H), 1.66 (dm, J=13.2 Hz, 1H), 1.37 (qt, J=12.9 Hz, 3.2 Hz, 2H), 1.30 (qd, J=12.4 Hz, 3.2 Hz, 2H), 1.06 (qt, J=12.9 Hz, 3.7 Hz, 1H).

Step 2: Phenyl-cyclohexyl-cyclopentadienyl-(2,7-di-tert-butylfluoren-9-yl)methane

To a solution of 26.0 g (93.38 mmol) of 2,7-di-tert-butylfluorene in 250 ml of THF cooled to −50° C. 38.4 ml (93.31 mmol) of 2.43 M ^(n)BuLi in hexanes was added in one portion. This mixture was stirred overnight at room temperature. To the resulting orange solution a solution of 22.09 g (93.46 mmol) of 6-phenyl-6-cyclohexylfulvene in 200 ml of THF was added at room temperature in one portion. After stirring overnight at room temperature the dark-red reaction mixture was cooled in an ice-bath and then quenched with a solution of 8.8 ml of 12 M HCl in 100 ml of water. The resulting orange mixture was diluted with 1000 ml of water and then extracted with 500 ml of ether. The organic layer was separated and dried over Na₂SO₄. Removal of the solvents under vacuum gave orange oil, which was dissolved in 250 ml of n-hexane, and the resulting solution was slowly evaporated in vacuo to volume ca. 50 ml. The obtained suspension was diluted with 200 ml of n-hexane and filtered off (G3) to give 33.17 g (69%) of 1-phenyl-1-cyclohexyl-1-cyclopentadienyl-1-(2,7-di-tert-butylfluorenyl)methane as a white powder.

Anal. calc. for C₃₉H₄₆: C, 90.99; H, 9.01. Found: C, 91.34; H, 9.38.

¹H NMR (CDCl₃): δ 8.18-6.16 (set of multiplets, sum 12H), 6.02-4.86 (set of singlets, sum 3H), 3.57-0.13 (set of singlets and multiplets, sum 31H).

Step 3: (Phenyl)cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dichloride

To a solution of 10.17 g (19.76 mmol) of 1-phenyl-1-cyclohexyl-1-cyclopentadienyl-1-(2,7-di-tert-butylfluoren-9-yl)methane in 250 ml of ether cooled to −78° C. 15.8 ml (39.5 mmol) of 2.5 M ^(n)BuLi in hexanes was added in one portion. This mixture was stirred overnight at room temperature. The resulting light-orange solution with orange precipitate was cooled to −50° C., and 6.33 g (19.76 mmol) of HfCl₄ was added. The formed mixture was stirred for 24 h at room temperature and then evaporated to dryness. The residue was stirred with 100 ml of warm toluene, the formed suspension was filtered through a glass frit (G4), and the filtrate was evaporated to ca. 35 ml. Precipitated overnight at room temperature white solid was filtered off (G4) and discarded. The mother liquor was evaporated to ca. 20 ml, and 20 ml of n-hexane was added to the residue. Yellow solid precipitated overnight at −30° C. was filtered off (G3) and dried in vacuo to give 3.20 g of (phenyl)(cyclohexyl)methylene (cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl) hafnium dichloride. The mother liquor was evaporated to dryness, and the residue was dissolved in 25 ml of n-hexane. Solid precipitated from this solution overnight at −30° C. was collected and dried in vacuo. This procedure gave additional 0.60 g of the target complex. Thus, the total yield of (phenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl) hafnium dichloride isolated in this synthesis was 3.80 g (25%).

Anal. calc. for C₃₉H₄₄Cl₂Hf: C, 61.46; H, 5.82. Found: C, 61.37; H, 6.10.

¹H NMR (CDCl₃): δ 8.02 (d, J=8.8 Hz, 1H), 7.95 (d, J=8.8 Hz, 1H), 7.76 (d, J=7.8 Hz, 1H), 7.68 (s, 1H), 7.63 (dd, J=8.8 Hz, J=1.2 Hz, 1H), 7.57-7.51 (m, 2H), 7.48 (dd, J=8.8 Hz, J=1.6 Hz, 1H), 7.45-7.41 (m, 1H), 7.39 (ddd, J=7.5 Hz, J=7.5 Hz, J=1.0 Hz, 1H), 6.36-6.31 (m, 1H), 6.21-6.16 (m, 1H), 5.96 (s, 1H), 5.76-5.71 (m, 1H), 5.55-5.50 (m, 1H), 3.26 (t, J=11.5 Hz, 1H), 2.33 (d, J=12.9 Hz, 1H), 2.14 (d, J=12.3 Hz, 1H), 1.94-1.83 (m, 2H), 1.16 (d, J=13.2 Hz, 1H), 1.66-1.56 (m, 1H), 1.53-1.40 (m, 1H), 1.41 (s, 9H), 1.40-1.30 (m, 1H), 1.12-1.01 (m, 1H), 0.96 (s, 9H), 0.91-0.79 (m, 1H).

Step 4: (Phenyl)cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl

To a solution of 3.80 g (4.99 mmol) of (phenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dichloride in a mixture of 50 ml of toluene and 50 ml of ether 7.0 ml (14.77 mmol) of 2.11 M MeMgBr in ether was added. The resulting mixture was refluxed for 30 min and then evaporated to ca. 25 ml. The obtained mixture was heated to 80-90° C. and filtered while hot through glass frit (G4) to remove insoluble magnesium salts. The filter cake was additionally washed with 5×20 ml of warm n-hexane. The combined filtrate was evaporated almost to dryness, and then 20 ml of n-hexane was added to the residue. The resulting mixture was filtered once again through a glass frit (G4). The mother liquor was evaporated to dryness, and the residue was dissolved in 7 ml of n-hexane. Yellow powder precipitated from this solution overnight at −30° C. was collected and dried in vacuum.

This procedure gave 3.05 g (88%) of pure (phenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl.

Anal. calc. for C₄₁H₅₀Hf: C, 68.27; H, 6.99. Found: C, 68.49; H, 7.22.

¹H NMR (CDCl₃): δ 8.08 (d, J=8.6 Hz, 1H), 7.98 (d, J=8.9 Hz, 1H), 7.73 (d, J=7.6 Hz, 1H), 7.58-7.48 (m, 3H), 7.45 (td, J=7.6 Hz, J=1.5 Hz, 1H), 7.38-7.28 (m, 3H), 6.28-6.21 (m, 1H), 6.12-6.06 (m, 1H), 5.86 (s, 1H), 5.62-5.55 (m, 1H), 5.33-5.27 (m, 1H), 3.06 (t, J=11.5 Hz, 1H), 2.28 (d, J=12.8 Hz, 1H), 2.10 (d, J=12.3 Hz, 1H), 1.90-1.75 (m, 2H), 1.70 (d, J=13.3 Hz, 1H), 1.65-1.20 (m, 1H), 1.48-1.33 (m, 1H), 1.40 (s, 9H), 1.31-1.16 (m, 1H), 1.08-0.92 (m, 1H), 0.95 (s, 9H), 0.77-0.62 (m, 1H), −1.79 (s, 3H), −1.93 (s, 3H). ¹³C{¹H} NMR (CDCl₃,): δ 150.30, 147.62, 140.00, 132.05, 129.17, 127.31, 126.95, 126.75, 124.03, 123.70, 122.93, 122.79, 120.91, 120.54, 119.29, 117.90, 116.35, 115.93, 112.41, 111.17, 109.62, 101.41, 99.72, 76.78, 57.85, 43.58, 38.06, 37.13, 35.47, 34.72, 31.56, 30.72, 29.02, 28.27, 27.36, 26.91, 26.70.

Complex 3 (C3):

(Phenyl)isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl Step 1: 6-Isopropyl-6-phenylfulvene

To a solution of 14.82 g (100 mmol) of isopropyl phenyl ketone in 40 ml of THF cooled in an ice-bath a solution of 20.3 g (120 mmol, 1.2 equiv.) of cyclopentadienylmagnesium bromide in 120 ml of THF was added dropwise. The resulting mixture was refluxed for 3 h, then stirred overnight at room temperature, finally, cooled in an ice-bath and quenched with 10% HCl to pH˜5-6. This mixture was extracted with 3×150 ml of hexane, and the combined organic extract was dried over Na₂SO₄. Removal of the solvent under vacuum gave a dark-red oil. The product was isolated by flash-chromatography on silica gel 60 (40-63 μm; eluent: hexane). This procedure gave 8.32 g (42%) of 6-isopropyl-6-phenylfulvene as a light orange oil, which completely crystallized during storage at −30° C.

Anal. calc. for C₁₅H₁₆: C, 91.78; H, 8.22. Found: C, 92.00; H, 8.41.

¹H NMR (CDCl₃): δ 7.36-7.30 (m, 3H), 7.21-7.15 (m, 2H), 6.70 (ddd, J=5.3 Hz, J=1.9 Hz, J=1.5 Hz, 1H), 6.54 (ddd, J=5.3 Hz, J=1.9 Hz, J=1.5 Hz, 1H), 6.37 (ddd, J=5.3 Hz, J=1.9 Hz, J=1.5 Hz, 1H), 5.77 (ddd, J=5.3 Hz, J=1.9 Hz, J=1.5 Hz, 1H), 3.50 (sept, J=7.0 Hz, 1H), 1.14 (d, J=7.0 Hz, 6H). ¹³C{¹H} NMR (CDCl₃): δ 159.82, 143.03, 138.92, 132.14, 130.72, 129.20, 127.19, 126.98, 124.36, 120.22, 33.72, 22.13.

Step 2: (Phenyl)isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butyIfluoren-9-yl)hafnium dichloride

To a solution of 11.77 g (42.27 mmol) of 2,7-di-tert-butylfluorene in 250 ml of ether cooled to −50° C., 17.4 ml (42.28 mmol) of 2.43 M ^(n)BuLi in hexanes was added in one portion. This mixture was stirred overnight at room temperature. The resulting orange solution was cooled to −50° C., and a solution of 8.30 g (42.29 mmol) of 6-isopropyl-6-phenylfulvene in 150 ml of ether was added in one portion. After stirring overnight at room temperature the dark-red reaction mixture was cooled to −50° C., and 17.4 ml (42.28 mmol) of 2.43 M ^(n)BuLi in hexanes was added in one portion. This mixture was stirred overnight at room temperature. The resulting dark-red solution was cooled to −50° C., and 13.55 g (42.3 mmol) of HfCl₄ was added. The formed mixture was stirred for 24 h at room temperature, then it was evaporated to dryness, and the residue was treated with 150 ml of warm toluene. This mixture was filtered while hot through glass frit (G4), the filtrate was evaporated to ca. 50 ml, and 80 ml of n-hexane was added to the residue. Precipitated solid was filtered and discarded. The mother liquor was evaporated almost to dryness, and the residue was triturated with 70 ml of n-hexane. Orange-yellow precipitate was filtered to give 5.80 g (ca. 19%) of (phenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dichloride with ca. 90% purity. The analytically pure sample (2.51 g, 8%) was obtained by recrystallization of crude product from toluene.

Anal. calc. for C₃₆H₄₀Cl₂Hf: C, 59.88; H, 5.58. Found: C, 60.07; H, 5.73.

¹H NMR (CDCl₃): δ 8.01 (d, J=8.8 Hz, 1H), 7.95 (d, J=8.9 Hz, 1H), 7.78 (dm, J=7.8 Hz, 1H), 7.69 (s, 1H), 7.62 (d, J=8.9 Hz, 1H), 7.59-7.51 (m, 2H), 7.49 (dd, J=8.8 Hz, J=1.2 Hz, 1H), 7.47-7.36 (m, 2H), 6.37-6.30 (m, 1H), 6.22-6.16 (m, 1H), 5.99 (br.s, 1H), 5.75-5.69 (m, 1H), 5.57-5.51 (m, 1H), 3.69 (sept, J=6.7 Hz, 1H), 1.39 (s, 9H), 1.31 (d, J=6.7 Hz, 3H), 1.05 (d, J=6.7 Hz, 3H), 0.97 (s, 9H). ¹³C{¹H} NMR (CDCl₃,): δ 152.22, 149.49, 137.95, 131.85, 129.31, 127.77, 127.42, 124.11, 124.06, 123.96, 123.43, 122.28, 120.46, 119.93, 119.81, 118.99, 118.56, 118.52, 116.70, 115.03, 100.10, 99.06, 78.64, 58.17, 35.40, 34.84, 32.74, 31.11, 30.51, 18.34, 17.89.

Step 3: (Phenyl)isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-buty fluoren-9-yl)hafnium dimethyl

To a solution of 3.3 g (ca. 4.6 mmol) of crude (phenyl)(isopropyl)methylene(cyclo-pentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dichloride (residue after recrystallization from toluene) in a mixture of 30 ml of toluene and 15 ml of ether, 6.5 ml (17.55 mmol) of 2.7 M MeMgBr in ether was added. The resulting mixture was stirred overnight at room temperature. Most of ether was distilled off, and the resulting mixture was filtered through glass frit (G4) to remove insoluble magnesium salts. The filtrate was evaporated to ca. 15 ml and filtered again through glass frit (G4). The mother liquor was evaporated to ca. 5 ml, 15 ml of n-hexane was added, and the resulting slightly turbid solution was filtered through glass frit (G4). Yellow powder precipitated from the filtrate overnight at −30° C. was collected and dried in vacuum. This procedure gave 1.46 g (ca. 47%) of (phenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl) hafnium dimethyl.

Anal. calc. for C₃₈H₄₆Hf: C, 66.99; H, 6.81. Found: C, 67.14; H, 7.02.

¹H NMR (CDCl₃): δ 8.09 (d, J=8.8 Hz, 1H), 7.99 (d, J=8.8 Hz, 1H), 7.75 (dm, J=7.9 Hz, 1H), 7.57 (br.s, 1H), 7.56-7.44 (m, 3H), 7.39-7.29 (m, 3H), 6.27-6.23 (m, 1H), 6.13-6.08 (m, 1H), 5.88 (br.d, J=1.0 Hz, 1H), 5.59-5.55 (m, 1H), 5.33-5.29 (m, 1H), 3.55-3.43 (m, 1H), 1.38 (s, 9H), 1.22 (d, J=6.7 Hz, 3H), 0.97-0.93 (s and d, sum 12H), −1.79 (s, 3H), −1.92 (s, 3H).

Complex Elemental Analysis (ICP Method):

Complex Hf (%) purity Zr (%) impurity C1 99.61 0.39 C2 99.51 0.49

b) Preparation of Catalyst System and Polymerization

Comparative Examples: Procedure for MAO/TIBA as Cocatalyst

a. MAO/TIBA Preparation:

MAO/TIBA solutions are commercially available but can also be easily prepared.

TIBA (4.30 g, 2.17×10⁻² mol) was added to a solution of Chemtura MAO 30% wt in toluene (8.39 g, 4.34×10⁻² mol) in a Schott glass bottle placed in a glove box and dried several days at 160° C. prior to use. The mixture was then stirred at room temperature for one hour. The resulting clear colourless solution was stored in a glove box and further used as such (concentration: 3.42×10⁻³ mol Al/g).

b. Catalyst Activation:

The catalyst solution is prepared by dissolving the desired amount of complex into the MAO/TIBA solution to reach an AI/Hf molar ratio of 200. For all experiments the solution is aged overnight prior to injection into the reactor.

c. Polymerization Procedure

A 125 mL reactor is filled with the desired amount of solvent (isopar E), the scavenger (0.5 mmol of MAO/TiBA) and 1-octene. Solvent and monomers amounts are chosen to have an initial liquid volume of 80 mL at the polymerization conditions.

The reactor is then heated up and carefully pressurised with ethylene (25-28 bar-g). When conditions are stable the ethylene pressure is adjusted to 30 bar-g and the mixture is allowed to stir at 750 rpm during 10 minutes in order to determine the residual ethylene uptake.

After this time the catalytic solution (diluted with 4 mL of toluene) is injected and the pressure is kept constant by feeding ethylene. After 10 minutes of polymerization a killing agent (either EtOH or CO₂) is injected to quench the polymerization. Then the reactor is vented, the temperature decreased and then the vessel is opened and the solution discharged in an aluminium pan containing few milligrams (˜500 ppm related to the copolymer produced) of Irganox 1076. The pan is then placed under a well-ventilated fume hood until the volatiles are evaporated. The collected residual material is analysed by HT-SEC and DSC.

Inventive Examples: Procedure for TB or AB as Cocatalyst

Polymerization procedure is in general terms the same as for the MAO/TiBA case except for-Scavenger, TEA (0.035 or 0.35 mmoles) is used instead of MAO/TiBA

Catalyst (dissolved in 4 mL toluene) and cocatalyst (also dissolved in 4 mL toluene) solutions are not premixed but contacted in the injection line immediately prior the injection in the reactor.

All other operations are performed as described for the MAO/TiBA case.

TABLE 1 C2/C8 copolymerization results at 30 bar-g at 160° C. with different C8/C2 ratios, activator MAO/TiBA (2/1 molar, Al/Hf 200 molar) vs AB (B/Hf = 1.25 molar). Inventive Examples IE1-IE6 and Comparative Examples CE1-CE3 Average. C8 in C8/C2 ratio polymer Reactivity Productivity in solution (NMR) ratio C8/C2 GPC unit kg PE/g_(cat) Mw Ex Complex Cocatalyst in 10 min wt/wt % wt kDa PDI IE1 C1 AB 25.3 1.1 20.0 0.22 185 3.4 CE1 C1 MAO/TIBA 4.5 1.3 12.4 0.11 87 3.5 IE2 C1 AB 50.6 1.7 26.9 0.21 120 3.1 IE3 C2 AB 56.0 1.3 21.7 0.21 153 3.2 CE2 C2 MAO/TIBA 3.0 1.3 10.8 0.09 105 3.7 IE4 C2 AB 74.4 1.6 28.1 0.24 121 3.3 IE5 C3 AB 24.7 1.1 15.7 0.17 202 3.8 CE3 C3 MAO/TIBA 4.2 1.3 11.3 0.10 115 3.8 IE6 C3 AB 50.2 1.7 26.2 0.21 104 3.0

Table 1 shows the performance results of Complexes 1 to 3 using two activation methods MAO/TIBA (Comparative) and AB (Inventive) catalysts and different C8 feed. As is shown in Table 1 regarding activation, significant clear difference on the performance between the two activation methods has been observed.

-   -   The results shown in FIG. 1-3 indicate that the three bridged         Cp-Flu complexes 1 to 3 exhibit significantly higher activity,         molecular weight capability, and C8 reactivity in solution         ethylene/1-octene copolymerization when activated with borate AB         compared to MAO/TIBA.

Table 2 compares the activating performance of the AB (B/Hf=1.25 molar) and TB (B/Hf=1.24 molar) borate activators:

TABLE 2 Average. C8 in C8/C2 polymer Productivity ratio in (NMR or Reactivity kg PE/g_(cat) solution T_(g)) ratio GPC Ex Complex cocatalyst in 10 min wt/wt % wt C8/C2 Mw kDa PDI IE3 C2 AB 56.0 1.3 21.7 0.21 153 3.2 CE2 C2 MAO/TiBA 3.0 1.3 10.8 0.09 105 3.7 IE4 C2 AB 74.4 1.6 28.1 0.24 121 3.3 IE7 C2 TB 10.4 1.8 26.1 0.20 188 3.5 (Tg)

Table 3 shows the influence of the B/Hf molar ratio.

TABLE 3 Average. C8 in C8/C2 polymer Productivity ratio in (NMR B/Hf kg PE/g_(cat) solution or Tg) Reactivity GPC Ex Complex molar in 10 min wt/wt % wt ratio C8/C2 Mw kDa PDI IE8 C2 AB 1 74.8 1.6 28.6 0.25 121 3.0 (Tg) IE4 C2 AB 1.25 74.4 1.6 28.1 0.24 121 3.3 IE9 C2 AB 1.5 92.2 1.6 28.9 0.24 108 3.5 (Tg) CE4 C2 AB 2 25.6 1.7 25.5 0.20 153 3.1 (Tg)

The results indicate that the preferred B/Hf ratio is from 1 to less than 2 molar ratio.

In Table 4 the solubility of C0 and C2 complexes in hexane is shown.

TABLE 4 Soubility of hafnium complexes in hexane Complex Solubility at 25° C. [wt %] C0 2 C2 5.2

As is shown in Table 4, complex C2 has a higher solubility compared to complex C0. 

The invention claimed is:
 1. A catalyst system for producing ethylene copolymers in a high temperature solution process at temperatures higher than 100° C., the catalyst system comprising: (i) a metallocene complex of formula (I)

wherein M is Hf; each X is independently a C₁₋₆ alkyl, benzyl or a halogen atom; R's are the same or different and are independently selected from the group consisting of linear or branched C₁-C₁₀ alkyl; R¹ is phenyl, which is unsubstituted or substituted by one linear or branched C₁-C₁₀ alkyl group; and R² is a linear or cyclic C₃-C₂₀ alkyl group or a branched CR³R⁴R⁵ group, wherein R³ is hydrogen or a C₁-C₂₀ alkyl group and R⁴ and R⁵ are the same or are different and are independently a C₁-C₂₀ alkyl group; and (ii) a boron containing cocatalyst; wherein the catalyst system is a homogeneous or non-supported catalyst system.
 2. The catalyst system according to claim 1, wherein in the formula (I): R's are the same or different and are independently selected from the group consisting of linear or branched C₁-C₆ alkyl; R¹ is phenyl, which is unsubstituted or substituted by one linear or branched C₁-C₆ alkyl group; and R² is a linear or cyclic C₃-C₁₀ alkyl group or a branched CR³R⁴R⁵ group, wherein R³ is hydrogen and R⁴ and R⁵ are the same or are different and are independently a C₁-C₁₀ alkyl group.
 3. The catalyst system according to claim 2, wherein in the formula (I): R's are the same and are a linear or branched C₁-C₆ alkyl; R¹ is phenyl; and R² is a linear or cyclic C₅-C₁₀ alkyl group or a branched CR³R⁴R⁵ group, wherein R³ is hydrogen and R⁴ and R⁵ are the same or are different and are independently a C₁-C₃ alkyl group.
 4. The catalyst system according to claim 3, wherein in the formula (I): each X is independently a methyl, benzyl, or chloride group; R's are the same and are all methyl groups; and R² is i-propyl, n-hexyl, or cyclohexyl.
 5. The catalyst system according to claim 1, wherein the metallocene complex of formula (I) is (Phenyl)(cyclohexyl) methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dibenzyl; (Phenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; (Phenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dibenzyl; (Phenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; (Phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dibenzyl; (Phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; (Phenyl)(cyclopentyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dibenzyl; (Phenyl)(cyclopentyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; (para-isopropylphenyl)(cyclohexyl)methylene (cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dibenzyl; (para-isopropylphenyl) (cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; (para-isopropylphenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dibenzyl; (para-isopropylphenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; (para-isopropylphenyl)(1-hexyl)methylene (cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dibenzyl; (para-isopropylphenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; (para-isopropylphenyl)(cyclopentyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dibenzyl; or (para-isopropyl)(cyclopentyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl.
 6. The catalyst system as claimed in claim 1, wherein said boron containing cocatalyst comprises an anion of formula: (Z)₄ B ⁻  (II) where Z is an optionally substituted phenyl derivative, said substituent being a halo-C₁₋₆-alkyl or halide group.
 7. The catalyst system according to claim 1, wherein all R's are the same and are a linear or branched C₁-C₆ alkyl.
 8. The catalyst system according to claim 1, wherein: the catalyst system is prepared in solution by contacting the metallocene complex of Formula (I), as a solid or as a solution, with the cocatalyst in a hydrocarbon diluent or previously dissolved in an aromatic solvent, or the catalyst system is formed by sequentially adding the components of the catalyst system directly into a polymerization reactor.
 9. The catalyst system as claimed in claim 1, wherein said boron containing cocatalyst is selected from the group consisting of triphenylcarbeniumtetrakis (pentafluorophenyl) borate, N,N-dimethylcyclohexylammoniumtetrakis(pentafluorophenyl) borate, N,N-dimethylbenzylammoniumtetrakis(pentafluorophenyl)borate, and N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate.
 10. The catalyst system of claim 1, wherein in the formula (I) R's are the same and are all methyl groups.
 11. The catalyst system of claim 1, wherein in the formula (I) R² is i-propyl, n-hexyl, or cyclohexyl.
 12. The catalyst system of claim 1, wherein in the formula (I) R¹ is unsubstituted phenyl.
 13. The catalyst system of claim 1, wherein in the formula (I) each X is independently a methyl, benzyl, or chloride group.
 14. The catalyst system of claim 1, wherein the metallocene complex of formula (I) is (Phenyl)(cyclohexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; (Phenyl)(isopropyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl; or (Phenyl)(1-hexyl)methylene(cyclopentadienyl)(2,7-di-tert-butylfluoren-9-yl)hafnium dimethyl.
 15. The catalyst system of claim 1, wherein said boron containing cocatalyst comprises N,N-Dimethylanilinium Tetrakis(pentafluorophenyl)borate.
 16. The catalyst system of claim 1, wherein the metallocene complex of formula (I) and the boron containing cocatalyst are provided in a molar ratio of boron to Hf of 1:1 to 5:1 mol/mol.
 17. The catalyst system of claim 1, the metallocene complex of formula (I) and the boron containing cocatalyst are provided in a molar ratio of boron to Hf of 1:1 to less than 2:1 mol/mol. 